BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEMORY LENS

    MDR report key: 285806 · Received July 17, 2000

    Report

    Report Number
    2648166-2000-00167
    Event Type
    Injury
    Date Received
    July 17, 2000
    Report Date
    July 17, 2000
    Manufacturer
    CIBA VISION
    Product Code
    HQL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED ON 05/23/2000 THAT, "A PATIENT HAD KERATIC PRECIPITATES TREATED WITH STEROIDS. LENS WAS REMOVED EIGHT WEEKS POST OP." AN ADVERSE REACTION REPORT WAS NOT COMPLETED BY REPORTING PHYSICIAN AND THEREFORE NO OTHER DETAILS ARE KNOWN. FOLLOW-UP WAS MADE ON FOUR ADDITIONAL OCCASIONS FOLLOWING THE INITIAL CONTACT."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEMORY LENS INTRAOCULAR LENS HQL CIBA VISION NI *

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO